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Details

Stereochemistry ACHIRAL
Molecular Formula C20H23N5S.ClH
Molecular Weight 401.956
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of Timegadine hydrochloride

SMILES

Cl.CC1=NC2=C(C=CC=C2)C(N\C(NC3=NC=CS3)=N/C4CCCCC4)=C1

InChI

InChIKey=IWMWBGDREQGECL-UHFFFAOYSA-N
InChI=1S/C20H23N5S.ClH/c1-14-13-18(16-9-5-6-10-17(16)22-14)24-19(25-20-21-11-12-26-20)23-15-7-3-2-4-8-15;/h5-6,9-13,15H,2-4,7-8H2,1H3,(H2,21,22,23,24,25);1H

HIDE SMILES / InChI
Timegadine Is a quinolylguanidine derivative patented by Loevens Kemiske Fabrik Produktionsaktieselskab as an anti-arthritic agent. Timegadine acts as a potent, competitive inhibitor of cyclo-oxygenase and lipo-oxygenase. Timegadine significantly inhibits both the primary and secondary lesions of rats adjuvant arthritis when the treatment is initiated on the day of the disease induction and continues for 28 days. Timegadine is able specifically to prevent the development of the swelling of the non-injected paw until 28 days after the adjuvant injection when administered for 5 days prior to and 5 days after the induction of the disease, in analogy with the effect of cyclophosphamide. In clinical trials, Timegadine significantly improves both biochemical and clinical markers of disease activity, i.e. ESR, serum IgG and IgM, leukocyte and platelet counts, duration of morning stiffness, Ritchie index, number of swollen joints and pain. Timegadine treatment associated with gastrointestinal and allergic side effects.

Approval Year

PubMed

PubMed

TitleDatePubMed
Timegadine: more than a non-steroidal for the treatment of rheumatoid arthritis. A controlled, double-blind study.
1988
Patents

Sample Use Guides

500 mg/day
Route of Administration: Oral
Name Type Language
Timegadine hydrochloride
Common Name English
SR-1368 HYDROCHLORIDE
Common Name English
SR 1368 HYDROCHLORIDE
Common Name English
N-CYCLOHEXYL-N'-(2-METHYL-4-QUINOLINEYL)-N''-THIAZOL-2-YLGUANIDINEMONOHYDROCHLORIDE
Common Name English
Code System Code Type Description
PUBCHEM
44151069
Created by admin on Sat Dec 16 20:08:41 GMT 2023 , Edited by admin on Sat Dec 16 20:08:41 GMT 2023
PRIMARY
FDA UNII
98HR33CND7
Created by admin on Sat Dec 16 20:08:41 GMT 2023 , Edited by admin on Sat Dec 16 20:08:41 GMT 2023
PRIMARY
ECHA (EC/EINECS)
275-185-6
Created by admin on Sat Dec 16 20:08:41 GMT 2023 , Edited by admin on Sat Dec 16 20:08:41 GMT 2023
PRIMARY
EPA CompTox
DTXSID30221302
Created by admin on Sat Dec 16 20:08:41 GMT 2023 , Edited by admin on Sat Dec 16 20:08:41 GMT 2023
PRIMARY
CAS
71080-06-3
Created by admin on Sat Dec 16 20:08:41 GMT 2023 , Edited by admin on Sat Dec 16 20:08:41 GMT 2023
PRIMARY